# SODIUM POLYSTYRENE SULFONATE

NDC: 71335-2855
Generic name: sodium polystyrene sulfonate
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL, RECTAL
Marketing started: 20170124

FDA application: ANDA204071

## Active ingredients

- SODIUM POLYSTYRENE SULFONATE: 4.1 meq/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d6016e9d-dec6-4f14-b10b-7ec1aba3964a